Matijević, Borko M.

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c40d6b9e-466a-44a1-b086-25357b63b189
  • Matijević, Borko M. (5)
  • Matijević, Borko (2)
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Synthesis, physicochemical characterization, and TD–DFT calculations of monothiocarbohydrazone derivatives

Mrđan, Gorana S.; Vastag, Gyöngyi Gy.; Škorić, Dušan Đ.; Radanović, Mirjana M.; Verbić, Tatjana; Milčić, Miloš K.; Stojiljković, Ivana N.; Marković, Olivera S.; Matijević, Borko M.

(Springer Nature, 2021)

TY  - JOUR
AU  - Mrđan, Gorana S.
AU  - Vastag, Gyöngyi Gy.
AU  - Škorić, Dušan Đ.
AU  - Radanović, Mirjana M.
AU  - Verbić, Tatjana
AU  - Milčić, Miloš K.
AU  - Stojiljković, Ivana N.
AU  - Marković, Olivera S.
AU  - Matijević, Borko M.
PY  - 2021
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4453
AB  - Derivatives of thiocarbohydrazone studied so far have shown great biological activity such as antioxidant, antimicrobial, and anticancer. Most of these compounds are bis-substituted derivatives, while monothiocarbohydrazones are much less investigated. Еighteen monothiocarbohydrazones were synthesized and subjected to physicochemical characterization in order to facilitate the examination of their potential biological activity and application in future studies. The structure of synthesized derivatives was confirmed with NMR and FT–IR spectroscopy, and with elemental analysis. For one of the compounds, single-crystal X-ray diffraction analysis was performed. Specific and non-specific molecular interactions were interpreted by LSER principles, using Catalan’s model. For additional information about the dominance and influence of the interactions presented, correlations with Hansen’s solubility parameters were calculated. Influence of the type and position of the substituent on absorption maxima was determined with LFER (linear free-energy relationship) principles, using Hammett’s equation. Acidity constants of the synthesized compounds were theoretically calculated and experimentally determined. Moreover, the excitation of a molecule by a photon of UV–Vis light was interpreted by time-dependent density functional theory (TD–DFT) calculations of UV absorption bands, and intramolecular charge transfer (ICT) was quantified by calculations of the charge transfer distances (DCT). © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.
PB  - Springer Nature
T2  - Structural Chemistry
T2  - Structural Chemistry
T2  - Structural Chemistry
T1  - Synthesis, physicochemical characterization, and TD–DFT calculations of monothiocarbohydrazone derivatives
VL  - 32
IS  - 3
SP  - 1231
EP  - 1245
DO  - 10.1007/s11224-020-01700-y
ER  - 
@article{
author = "Mrđan, Gorana S. and Vastag, Gyöngyi Gy. and Škorić, Dušan Đ. and Radanović, Mirjana M. and Verbić, Tatjana and Milčić, Miloš K. and Stojiljković, Ivana N. and Marković, Olivera S. and Matijević, Borko M.",
year = "2021",
abstract = "Derivatives of thiocarbohydrazone studied so far have shown great biological activity such as antioxidant, antimicrobial, and anticancer. Most of these compounds are bis-substituted derivatives, while monothiocarbohydrazones are much less investigated. Еighteen monothiocarbohydrazones were synthesized and subjected to physicochemical characterization in order to facilitate the examination of their potential biological activity and application in future studies. The structure of synthesized derivatives was confirmed with NMR and FT–IR spectroscopy, and with elemental analysis. For one of the compounds, single-crystal X-ray diffraction analysis was performed. Specific and non-specific molecular interactions were interpreted by LSER principles, using Catalan’s model. For additional information about the dominance and influence of the interactions presented, correlations with Hansen’s solubility parameters were calculated. Influence of the type and position of the substituent on absorption maxima was determined with LFER (linear free-energy relationship) principles, using Hammett’s equation. Acidity constants of the synthesized compounds were theoretically calculated and experimentally determined. Moreover, the excitation of a molecule by a photon of UV–Vis light was interpreted by time-dependent density functional theory (TD–DFT) calculations of UV absorption bands, and intramolecular charge transfer (ICT) was quantified by calculations of the charge transfer distances (DCT). © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.",
publisher = "Springer Nature",
journal = "Structural Chemistry, Structural Chemistry, Structural Chemistry",
title = "Synthesis, physicochemical characterization, and TD–DFT calculations of monothiocarbohydrazone derivatives",
volume = "32",
number = "3",
pages = "1231-1245",
doi = "10.1007/s11224-020-01700-y"
}
Mrđan, G. S., Vastag, G. Gy., Škorić, D. Đ., Radanović, M. M., Verbić, T., Milčić, M. K., Stojiljković, I. N., Marković, O. S.,& Matijević, B. M.. (2021). Synthesis, physicochemical characterization, and TD–DFT calculations of monothiocarbohydrazone derivatives. in Structural Chemistry
Springer Nature., 32(3), 1231-1245.
https://doi.org/10.1007/s11224-020-01700-y
Mrđan GS, Vastag GG, Škorić DĐ, Radanović MM, Verbić T, Milčić MK, Stojiljković IN, Marković OS, Matijević BM. Synthesis, physicochemical characterization, and TD–DFT calculations of monothiocarbohydrazone derivatives. in Structural Chemistry. 2021;32(3):1231-1245.
doi:10.1007/s11224-020-01700-y .
Mrđan, Gorana S., Vastag, Gyöngyi Gy., Škorić, Dušan Đ., Radanović, Mirjana M., Verbić, Tatjana, Milčić, Miloš K., Stojiljković, Ivana N., Marković, Olivera S., Matijević, Borko M., "Synthesis, physicochemical characterization, and TD–DFT calculations of monothiocarbohydrazone derivatives" in Structural Chemistry, 32, no. 3 (2021):1231-1245,
https://doi.org/10.1007/s11224-020-01700-y . .
9
1
8
7

Supplementary data for the article: Mrđan, G. S.; Vastag, G. G.; Škorić, D. Đ.; Radanović, M. M.; Verbić, T. Ž.; Milčić, M. K.; Stojiljković, I. N.; Marković, O. S.; Matijević, B. M. Synthesis, Physicochemical Characterization, and TD–DFT Calculations of Monothiocarbohydrazone Derivatives. Structural Chemistry 2021, 32 (3), 1231–1245. https://doi.org/10.1007/s11224-020-01700-y.

Mrđan, Gorana S.; Vastag, Gyöngyi Gy.; Škorić, Dušan Đ.; Radanović, Mirjana M.; Verbić, Tatjana; Milčić, Miloš K.; Stojiljković, Ivana N.; Marković, Olivera S.; Matijević, Borko M.

(Springer Nature, 2021)

TY  - DATA
AU  - Mrđan, Gorana S.
AU  - Vastag, Gyöngyi Gy.
AU  - Škorić, Dušan Đ.
AU  - Radanović, Mirjana M.
AU  - Verbić, Tatjana
AU  - Milčić, Miloš K.
AU  - Stojiljković, Ivana N.
AU  - Marković, Olivera S.
AU  - Matijević, Borko M.
PY  - 2021
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4454
PB  - Springer Nature
T2  - Structural Chemistry
T1  - Supplementary data for the article: Mrđan, G. S.; Vastag, G. G.; Škorić, D. Đ.; Radanović, M. M.; Verbić, T. Ž.; Milčić, M. K.; Stojiljković, I. N.; Marković, O. S.; Matijević, B. M. Synthesis, Physicochemical Characterization, and TD–DFT Calculations of Monothiocarbohydrazone Derivatives. Structural Chemistry 2021, 32 (3), 1231–1245. https://doi.org/10.1007/s11224-020-01700-y.
UR  - https://hdl.handle.net/21.15107/rcub_cherry_4454
ER  - 
@misc{
author = "Mrđan, Gorana S. and Vastag, Gyöngyi Gy. and Škorić, Dušan Đ. and Radanović, Mirjana M. and Verbić, Tatjana and Milčić, Miloš K. and Stojiljković, Ivana N. and Marković, Olivera S. and Matijević, Borko M.",
year = "2021",
publisher = "Springer Nature",
journal = "Structural Chemistry",
title = "Supplementary data for the article: Mrđan, G. S.; Vastag, G. G.; Škorić, D. Đ.; Radanović, M. M.; Verbić, T. Ž.; Milčić, M. K.; Stojiljković, I. N.; Marković, O. S.; Matijević, B. M. Synthesis, Physicochemical Characterization, and TD–DFT Calculations of Monothiocarbohydrazone Derivatives. Structural Chemistry 2021, 32 (3), 1231–1245. https://doi.org/10.1007/s11224-020-01700-y.",
url = "https://hdl.handle.net/21.15107/rcub_cherry_4454"
}
Mrđan, G. S., Vastag, G. Gy., Škorić, D. Đ., Radanović, M. M., Verbić, T., Milčić, M. K., Stojiljković, I. N., Marković, O. S.,& Matijević, B. M.. (2021). Supplementary data for the article: Mrđan, G. S.; Vastag, G. G.; Škorić, D. Đ.; Radanović, M. M.; Verbić, T. Ž.; Milčić, M. K.; Stojiljković, I. N.; Marković, O. S.; Matijević, B. M. Synthesis, Physicochemical Characterization, and TD–DFT Calculations of Monothiocarbohydrazone Derivatives. Structural Chemistry 2021, 32 (3), 1231–1245. https://doi.org/10.1007/s11224-020-01700-y.. in Structural Chemistry
Springer Nature..
https://hdl.handle.net/21.15107/rcub_cherry_4454
Mrđan GS, Vastag GG, Škorić DĐ, Radanović MM, Verbić T, Milčić MK, Stojiljković IN, Marković OS, Matijević BM. Supplementary data for the article: Mrđan, G. S.; Vastag, G. G.; Škorić, D. Đ.; Radanović, M. M.; Verbić, T. Ž.; Milčić, M. K.; Stojiljković, I. N.; Marković, O. S.; Matijević, B. M. Synthesis, Physicochemical Characterization, and TD–DFT Calculations of Monothiocarbohydrazone Derivatives. Structural Chemistry 2021, 32 (3), 1231–1245. https://doi.org/10.1007/s11224-020-01700-y.. in Structural Chemistry. 2021;.
https://hdl.handle.net/21.15107/rcub_cherry_4454 .
Mrđan, Gorana S., Vastag, Gyöngyi Gy., Škorić, Dušan Đ., Radanović, Mirjana M., Verbić, Tatjana, Milčić, Miloš K., Stojiljković, Ivana N., Marković, Olivera S., Matijević, Borko M., "Supplementary data for the article: Mrđan, G. S.; Vastag, G. G.; Škorić, D. Đ.; Radanović, M. M.; Verbić, T. Ž.; Milčić, M. K.; Stojiljković, I. N.; Marković, O. S.; Matijević, B. M. Synthesis, Physicochemical Characterization, and TD–DFT Calculations of Monothiocarbohydrazone Derivatives. Structural Chemistry 2021, 32 (3), 1231–1245. https://doi.org/10.1007/s11224-020-01700-y." in Structural Chemistry (2021),
https://hdl.handle.net/21.15107/rcub_cherry_4454 .

Investigation of physicochemical properties and potential biological activity of 2-pyridine-(thio)carbohydrazone derivatives

Mrđan, Gorana; Vaštag, Đenđi; Apostolov, Suzana; Rašeta, Milena; Verbić, Tatjana; Marković, Olivera S.; Matijević, Borko

(2021)

TY  - CONF
AU  - Mrđan, Gorana
AU  - Vaštag, Đenđi
AU  - Apostolov, Suzana
AU  - Rašeta, Milena
AU  - Verbić, Tatjana
AU  - Marković, Olivera S.
AU  - Matijević, Borko
PY  - 2021
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5963
AB  - Carbohydrazones and their thio analogs represent compounds obtained
by condensation of carbohydrazide and thiocarbohydrazide with carbonyl
compounds. Due to their structure, relatively simple synthesis, and high reactivity,
mentioned derivatives have a wide range of applications in all fields. In this study,
ionization constants of four newly synthesized mono(thio)carbohydrazones were
determined by applying the potentiometric method. Also, the influence of specific
and nonspecific intermolecular interactions on maxima shifting in UV-Vis absorption
spectra was investigated and quantified using the linear solvation energy relationships
method and Catalan’s model. Finally, by applying the DPPH assay, the
antioxidant potential of the newly synthesized compounds was determined, and thiocarbohydrazone
derivatives proved to be significantly more active when compared
to carbohydrazones.
C3  - XIV International Scientific Conference Contemporary Materials 2021 Programme and the Book of Abstracts, Banja Luka, September 9th to 10th, 2021
T1  - Investigation of physicochemical properties and potential biological activity of 2-pyridine-(thio)carbohydrazone derivatives
SP  - 40
EP  - 40
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5963
ER  - 
@conference{
author = "Mrđan, Gorana and Vaštag, Đenđi and Apostolov, Suzana and Rašeta, Milena and Verbić, Tatjana and Marković, Olivera S. and Matijević, Borko",
year = "2021",
abstract = "Carbohydrazones and their thio analogs represent compounds obtained
by condensation of carbohydrazide and thiocarbohydrazide with carbonyl
compounds. Due to their structure, relatively simple synthesis, and high reactivity,
mentioned derivatives have a wide range of applications in all fields. In this study,
ionization constants of four newly synthesized mono(thio)carbohydrazones were
determined by applying the potentiometric method. Also, the influence of specific
and nonspecific intermolecular interactions on maxima shifting in UV-Vis absorption
spectra was investigated and quantified using the linear solvation energy relationships
method and Catalan’s model. Finally, by applying the DPPH assay, the
antioxidant potential of the newly synthesized compounds was determined, and thiocarbohydrazone
derivatives proved to be significantly more active when compared
to carbohydrazones.",
journal = "XIV International Scientific Conference Contemporary Materials 2021 Programme and the Book of Abstracts, Banja Luka, September 9th to 10th, 2021",
title = "Investigation of physicochemical properties and potential biological activity of 2-pyridine-(thio)carbohydrazone derivatives",
pages = "40-40",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5963"
}
Mrđan, G., Vaštag, Đ., Apostolov, S., Rašeta, M., Verbić, T., Marković, O. S.,& Matijević, B.. (2021). Investigation of physicochemical properties and potential biological activity of 2-pyridine-(thio)carbohydrazone derivatives. in XIV International Scientific Conference Contemporary Materials 2021 Programme and the Book of Abstracts, Banja Luka, September 9th to 10th, 2021, 40-40.
https://hdl.handle.net/21.15107/rcub_cherry_5963
Mrđan G, Vaštag Đ, Apostolov S, Rašeta M, Verbić T, Marković OS, Matijević B. Investigation of physicochemical properties and potential biological activity of 2-pyridine-(thio)carbohydrazone derivatives. in XIV International Scientific Conference Contemporary Materials 2021 Programme and the Book of Abstracts, Banja Luka, September 9th to 10th, 2021. 2021;:40-40.
https://hdl.handle.net/21.15107/rcub_cherry_5963 .
Mrđan, Gorana, Vaštag, Đenđi, Apostolov, Suzana, Rašeta, Milena, Verbić, Tatjana, Marković, Olivera S., Matijević, Borko, "Investigation of physicochemical properties and potential biological activity of 2-pyridine-(thio)carbohydrazone derivatives" in XIV International Scientific Conference Contemporary Materials 2021 Programme and the Book of Abstracts, Banja Luka, September 9th to 10th, 2021 (2021):40-40,
https://hdl.handle.net/21.15107/rcub_cherry_5963 .

Determination of ionization constants of selected monocarbohydrazone derivatives

Mrđan, Gorana; Verbić, Tatjana; Marković, Olivera S.; Matijević, Borko; Vaštag, Đenđi; Apostolov, Suzana

(2020)

TY  - CONF
AU  - Mrđan, Gorana
AU  - Verbić, Tatjana
AU  - Marković, Olivera S.
AU  - Matijević, Borko
AU  - Vaštag, Đenđi
AU  - Apostolov, Suzana
PY  - 2020
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5960
AB  - Carbohydrazone derivatives represent a very significant class of compounds due to their wide biological activity. Ionization states of functional groups present in the molecule are of vital importance for understanding of the pharmacokinetic and pharmacodynamic properties of the newly synthesized com-pounds.
One of the physicochemical parameters, the ionization constant (pKa), can be used as a molecular descriptor in order to relate structure and activity of a com-pound, which may indicate further potential application of newly synthesized deri-vatives.
In this work, ionization constants of twenty monocarbohydrazone deriva-tives were determined using potentiometric method, in order to obtain information about their ionization states under certain conditions.
C3  - XIII International Scientific Conference Contemporary Materials 2020  Programme  and the Book of Abstracts, Banja Luka, 11th September, 2020
T1  - Determination of ionization constants of selected monocarbohydrazone derivatives
SP  - 50
EP  - 50
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5960
ER  - 
@conference{
author = "Mrđan, Gorana and Verbić, Tatjana and Marković, Olivera S. and Matijević, Borko and Vaštag, Đenđi and Apostolov, Suzana",
year = "2020",
abstract = "Carbohydrazone derivatives represent a very significant class of compounds due to their wide biological activity. Ionization states of functional groups present in the molecule are of vital importance for understanding of the pharmacokinetic and pharmacodynamic properties of the newly synthesized com-pounds.
One of the physicochemical parameters, the ionization constant (pKa), can be used as a molecular descriptor in order to relate structure and activity of a com-pound, which may indicate further potential application of newly synthesized deri-vatives.
In this work, ionization constants of twenty monocarbohydrazone deriva-tives were determined using potentiometric method, in order to obtain information about their ionization states under certain conditions.",
journal = "XIII International Scientific Conference Contemporary Materials 2020  Programme  and the Book of Abstracts, Banja Luka, 11th September, 2020",
title = "Determination of ionization constants of selected monocarbohydrazone derivatives",
pages = "50-50",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5960"
}
Mrđan, G., Verbić, T., Marković, O. S., Matijević, B., Vaštag, Đ.,& Apostolov, S.. (2020). Determination of ionization constants of selected monocarbohydrazone derivatives. in XIII International Scientific Conference Contemporary Materials 2020  Programme  and the Book of Abstracts, Banja Luka, 11th September, 2020, 50-50.
https://hdl.handle.net/21.15107/rcub_cherry_5960
Mrđan G, Verbić T, Marković OS, Matijević B, Vaštag Đ, Apostolov S. Determination of ionization constants of selected monocarbohydrazone derivatives. in XIII International Scientific Conference Contemporary Materials 2020  Programme  and the Book of Abstracts, Banja Luka, 11th September, 2020. 2020;:50-50.
https://hdl.handle.net/21.15107/rcub_cherry_5960 .
Mrđan, Gorana, Verbić, Tatjana, Marković, Olivera S., Matijević, Borko, Vaštag, Đenđi, Apostolov, Suzana, "Determination of ionization constants of selected monocarbohydrazone derivatives" in XIII International Scientific Conference Contemporary Materials 2020  Programme  and the Book of Abstracts, Banja Luka, 11th September, 2020 (2020):50-50,
https://hdl.handle.net/21.15107/rcub_cherry_5960 .

Synthesis, solvent interactions and computational study of monocarbohydrazones

Mrđan, Gorana S.; Matijević, Borko M.; Vastag, Gyöngyi Gy.; Božić, Aleksandra R.; Marinković, Aleksandar; Milčić, Miloš K.; Stojiljković, Ivana N.

(2020)

TY  - JOUR
AU  - Mrđan, Gorana S.
AU  - Matijević, Borko M.
AU  - Vastag, Gyöngyi Gy.
AU  - Božić, Aleksandra R.
AU  - Marinković, Aleksandar
AU  - Milčić, Miloš K.
AU  - Stojiljković, Ivana N.
PY  - 2020
UR  - https://doi.org/10.1007/s11696-020-01106-4
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4280
AB  - Carbohydrazones are compounds that are increasingly studied due to their wide potential biological activity. Monocarbohydrazones (mCHs), as one of the carbohydrazone derivatives, so far have been poorly investigated. For a more detailed study, in this paper, eighteen compounds of monocarbohydrazones (eight known and ten newly synthesized derivatives) were synthesized and characterized using NMR and IR spectroscopy. As carbohydrazones show E/Z isomerization caused by the presence of the imino group, some of the synthesized mCHs are in the form of a mixture of these two isomers. The effects of specific and nonspecific solvent–solute interactions on the UV absorption maxima shifts were evaluated using linear free energy relationships principles, i.e., using Kamlet–Taft’s and Catalan’s models. For more information about interactions between dissolved substance and the surrounding medium, correlations have been made with Hansen’s solubility parameters. The influence of the structure on the spectral behavior of the compounds tested was interpreted using Hammett’s equation. Experimentally obtained physicochemical properties of mCHs were compared to and confirmed with computational methods that included TD-DFT calculations and MP2 geometry optimizations.
T2  - Chemical Papers
T1  - Synthesis, solvent interactions and computational study of monocarbohydrazones
VL  - 74
IS  - 8
SP  - 2653
EP  - 2674
DO  - 10.1007/s11696-020-01106-4
ER  - 
@article{
author = "Mrđan, Gorana S. and Matijević, Borko M. and Vastag, Gyöngyi Gy. and Božić, Aleksandra R. and Marinković, Aleksandar and Milčić, Miloš K. and Stojiljković, Ivana N.",
year = "2020",
abstract = "Carbohydrazones are compounds that are increasingly studied due to their wide potential biological activity. Monocarbohydrazones (mCHs), as one of the carbohydrazone derivatives, so far have been poorly investigated. For a more detailed study, in this paper, eighteen compounds of monocarbohydrazones (eight known and ten newly synthesized derivatives) were synthesized and characterized using NMR and IR spectroscopy. As carbohydrazones show E/Z isomerization caused by the presence of the imino group, some of the synthesized mCHs are in the form of a mixture of these two isomers. The effects of specific and nonspecific solvent–solute interactions on the UV absorption maxima shifts were evaluated using linear free energy relationships principles, i.e., using Kamlet–Taft’s and Catalan’s models. For more information about interactions between dissolved substance and the surrounding medium, correlations have been made with Hansen’s solubility parameters. The influence of the structure on the spectral behavior of the compounds tested was interpreted using Hammett’s equation. Experimentally obtained physicochemical properties of mCHs were compared to and confirmed with computational methods that included TD-DFT calculations and MP2 geometry optimizations.",
journal = "Chemical Papers",
title = "Synthesis, solvent interactions and computational study of monocarbohydrazones",
volume = "74",
number = "8",
pages = "2653-2674",
doi = "10.1007/s11696-020-01106-4"
}
Mrđan, G. S., Matijević, B. M., Vastag, G. Gy., Božić, A. R., Marinković, A., Milčić, M. K.,& Stojiljković, I. N.. (2020). Synthesis, solvent interactions and computational study of monocarbohydrazones. in Chemical Papers, 74(8), 2653-2674.
https://doi.org/10.1007/s11696-020-01106-4
Mrđan GS, Matijević BM, Vastag GG, Božić AR, Marinković A, Milčić MK, Stojiljković IN. Synthesis, solvent interactions and computational study of monocarbohydrazones. in Chemical Papers. 2020;74(8):2653-2674.
doi:10.1007/s11696-020-01106-4 .
Mrđan, Gorana S., Matijević, Borko M., Vastag, Gyöngyi Gy., Božić, Aleksandra R., Marinković, Aleksandar, Milčić, Miloš K., Stojiljković, Ivana N., "Synthesis, solvent interactions and computational study of monocarbohydrazones" in Chemical Papers, 74, no. 8 (2020):2653-2674,
https://doi.org/10.1007/s11696-020-01106-4 . .
2
1
2
2

Supplementary data for article: Matijević, B. M.; Vaštag, T. T.; Apostolov, S. L.; Milčić, M. K.; Marinković, A. D.; Petrović, S. D. N-(Substituted Phenyl)-2-Chloroacetamides: LSER and LFER Study, 2015. https://doi.org/10.1016/j.arabjc.2015.09.008

Matijević, Borko M.; Vaštag, Đenđi Đ.; Apostolov, Suzana L.; Milčić, Miloš K.; Marinković, Aleksandar; Petrović, Slobodan D.

(2015)

TY  - DATA
AU  - Matijević, Borko M.
AU  - Vaštag, Đenđi Đ.
AU  - Apostolov, Suzana L.
AU  - Milčić, Miloš K.
AU  - Marinković, Aleksandar
AU  - Petrović, Slobodan D.
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3386
T2  - Arabian Journal of Chemistry
T1  - Supplementary data for article: Matijević, B. M.; Vaštag, T. T.; Apostolov, S. L.; Milčić, M. K.; Marinković, A. D.; Petrović, S. D. N-(Substituted Phenyl)-2-Chloroacetamides: LSER and LFER Study, 2015. https://doi.org/10.1016/j.arabjc.2015.09.008
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3386
ER  - 
@misc{
author = "Matijević, Borko M. and Vaštag, Đenđi Đ. and Apostolov, Suzana L. and Milčić, Miloš K. and Marinković, Aleksandar and Petrović, Slobodan D.",
year = "2015",
journal = "Arabian Journal of Chemistry",
title = "Supplementary data for article: Matijević, B. M.; Vaštag, T. T.; Apostolov, S. L.; Milčić, M. K.; Marinković, A. D.; Petrović, S. D. N-(Substituted Phenyl)-2-Chloroacetamides: LSER and LFER Study, 2015. https://doi.org/10.1016/j.arabjc.2015.09.008",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3386"
}
Matijević, B. M., Vaštag, Đ. Đ., Apostolov, S. L., Milčić, M. K., Marinković, A.,& Petrović, S. D.. (2015). Supplementary data for article: Matijević, B. M.; Vaštag, T. T.; Apostolov, S. L.; Milčić, M. K.; Marinković, A. D.; Petrović, S. D. N-(Substituted Phenyl)-2-Chloroacetamides: LSER and LFER Study, 2015. https://doi.org/10.1016/j.arabjc.2015.09.008. in Arabian Journal of Chemistry.
https://hdl.handle.net/21.15107/rcub_cherry_3386
Matijević BM, Vaštag ĐĐ, Apostolov SL, Milčić MK, Marinković A, Petrović SD. Supplementary data for article: Matijević, B. M.; Vaštag, T. T.; Apostolov, S. L.; Milčić, M. K.; Marinković, A. D.; Petrović, S. D. N-(Substituted Phenyl)-2-Chloroacetamides: LSER and LFER Study, 2015. https://doi.org/10.1016/j.arabjc.2015.09.008. in Arabian Journal of Chemistry. 2015;.
https://hdl.handle.net/21.15107/rcub_cherry_3386 .
Matijević, Borko M., Vaštag, Đenđi Đ., Apostolov, Suzana L., Milčić, Miloš K., Marinković, Aleksandar, Petrović, Slobodan D., "Supplementary data for article: Matijević, B. M.; Vaštag, T. T.; Apostolov, S. L.; Milčić, M. K.; Marinković, A. D.; Petrović, S. D. N-(Substituted Phenyl)-2-Chloroacetamides: LSER and LFER Study, 2015. https://doi.org/10.1016/j.arabjc.2015.09.008" in Arabian Journal of Chemistry (2015),
https://hdl.handle.net/21.15107/rcub_cherry_3386 .

N-(substituted phenyl)-2-chloroacetamides: LSER and LFER study

Matijević, Borko M.; Vaštag, Đenđi Đ.; Apostolov, Suzana L.; Milčić, Miloš K.; Marinković, Aleksandar; Petrović, Slobodan D.

(2015)

TY  - JOUR
AU  - Matijević, Borko M.
AU  - Vaštag, Đenđi Đ.
AU  - Apostolov, Suzana L.
AU  - Milčić, Miloš K.
AU  - Marinković, Aleksandar
AU  - Petrović, Slobodan D.
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/293
AB  - The UV absorption spectra of twelve. N-(substituted phenyl)-2-chloroacetamides were recorded in eighteen solvents. The effect of specific and non-specific solvent-solute interactions on the absorption maxima shifts was evaluated by using the Kamlet-Taft solvent parameter set,. i.e. applying linear solvation energy relationships (LSER) principles. Optimized geometries and experimental results were interpreted by using DFT (B3LYP/6-311+G(d,p) method) and time-dependent density functional (TD-DFT) method. Overall electron density in both ground and excited state was obtained by the use of Quantum Theory of Atoms in Molecules,. i.e. Bader's analysis. It was found that both solvent and substituents cause appropriate change of the extent of conjugation in the molecules that further affect their intra-molecular charge transfer (ICT) character. Linear free energy relationships (LFERs) were applied to the substituent-induced NMR chemical shifts (SCS) using single substituent parameter (SSP) and dual substituent parameter (DSP) model. Transmission mode of the electronic effects of substituent was discussed according to the results of theoretical calculations and results of LFER correlations. Comparative analysis of presented results with the ones published for structurally similar series of amide which contained cyano group, instead chlorine, provides additional information on the impact of present group to the properties of investigated compound.
T2  - Arabian Journal of Chemistry
T1  - N-(substituted phenyl)-2-chloroacetamides: LSER and LFER study
DO  - 10.1016/j.arabjc.2015.09.008
ER  - 
@article{
author = "Matijević, Borko M. and Vaštag, Đenđi Đ. and Apostolov, Suzana L. and Milčić, Miloš K. and Marinković, Aleksandar and Petrović, Slobodan D.",
year = "2015",
abstract = "The UV absorption spectra of twelve. N-(substituted phenyl)-2-chloroacetamides were recorded in eighteen solvents. The effect of specific and non-specific solvent-solute interactions on the absorption maxima shifts was evaluated by using the Kamlet-Taft solvent parameter set,. i.e. applying linear solvation energy relationships (LSER) principles. Optimized geometries and experimental results were interpreted by using DFT (B3LYP/6-311+G(d,p) method) and time-dependent density functional (TD-DFT) method. Overall electron density in both ground and excited state was obtained by the use of Quantum Theory of Atoms in Molecules,. i.e. Bader's analysis. It was found that both solvent and substituents cause appropriate change of the extent of conjugation in the molecules that further affect their intra-molecular charge transfer (ICT) character. Linear free energy relationships (LFERs) were applied to the substituent-induced NMR chemical shifts (SCS) using single substituent parameter (SSP) and dual substituent parameter (DSP) model. Transmission mode of the electronic effects of substituent was discussed according to the results of theoretical calculations and results of LFER correlations. Comparative analysis of presented results with the ones published for structurally similar series of amide which contained cyano group, instead chlorine, provides additional information on the impact of present group to the properties of investigated compound.",
journal = "Arabian Journal of Chemistry",
title = "N-(substituted phenyl)-2-chloroacetamides: LSER and LFER study",
doi = "10.1016/j.arabjc.2015.09.008"
}
Matijević, B. M., Vaštag, Đ. Đ., Apostolov, S. L., Milčić, M. K., Marinković, A.,& Petrović, S. D.. (2015). N-(substituted phenyl)-2-chloroacetamides: LSER and LFER study. in Arabian Journal of Chemistry.
https://doi.org/10.1016/j.arabjc.2015.09.008
Matijević BM, Vaštag ĐĐ, Apostolov SL, Milčić MK, Marinković A, Petrović SD. N-(substituted phenyl)-2-chloroacetamides: LSER and LFER study. in Arabian Journal of Chemistry. 2015;.
doi:10.1016/j.arabjc.2015.09.008 .
Matijević, Borko M., Vaštag, Đenđi Đ., Apostolov, Suzana L., Milčić, Miloš K., Marinković, Aleksandar, Petrović, Slobodan D., "N-(substituted phenyl)-2-chloroacetamides: LSER and LFER study" in Arabian Journal of Chemistry (2015),
https://doi.org/10.1016/j.arabjc.2015.09.008 . .
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